Congenital analbuminemia in a patient affected by hypercholesterolemia: A case report

BACKGROUND: Congenital analbuminemia (CAA) is a very rare disorder. Our data describes the clinical features and laboratory results of a new case established by mutation analysis of the albumin gene in a 39-year-old woman presenting with hypercholesterolemia. Our findings contribute to shed light on...

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Detalles Bibliográficos
Autores principales: Suppressa, Patrizia, Carbonara, Concetta, Lugani, Francesca, Campagnoli, Monica, Troiano, Teresa, Minchiotti, Lorenzo, Sabbà, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397822/
https://www.ncbi.nlm.nih.gov/pubmed/30842957
http://dx.doi.org/10.12998/wjcc.v7.i4.466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397822/
https://www.ncbi.nlm.nih.gov/pubmed/30842957
http://dx.doi.org/10.12998/wjcc.v7.i4.466

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